Clean Utility Professional

Found in: Talent DK C2 - 2 weeks ago


Søborg, Denmark Novo Nordisk AS Full time

Would you like to make an impact on aseptic pharma production with your clean utility expertise? Are you ready to make your knowledge operational for colleagues worldwide? 
Then this might be the position for you. Apply today and join us for a life-changing career


The position
Clean Utility plays a vital role in maintaining compliance in pharmaceutical production. As a department, we both support running production and new projects. We are responsible for the interaction between production processes and interpretation of external (GMP) requirements. We ensure global harmonization, and we actively participate in audits and inspections. We are also involved in the development and implementation of new technologies in Clean Utility systems. 
You will play an important role in ensuring the compliant and efficient operation of Novo Nordisk aseptic filling facilities world-wide. Your responsibilities will be to support our sites e.g., in Clean Utility projects, qualification, and troubleshooting.
 

A workday may include: 

Participation in troubleshooting and support in general.  Maintenance of global corporate documents and procedures.  Support in qualification of new water systems and improvements across the organization.

You will be cooperating with colleagues from different cultures, with different areas of expertise and at different organizational levels. You will be working out of Søborg, Denmark, but approximately 20-30 travel days may be expected.
There will be plenty of opportunities to take on new responsibilities and grow in this position.
 

Qualifications
To succeed in this role: 

You have a bachelor or master’s degree within mechanical engineering or equivalent.  You have minimum 3 years expertise within one or more areas of Clean Utility in aseptic production which could be from a pharmaceutical production site. You are used to and thrive working in a dynamic environment and can prioritize between many important tasks.  You have a high sense of quality. You have excellent communication skills and are fluent in written and spoken English. 

As a person, you are service minded, goal-oriented and a strong team player. You set pride in providing excellent support to colleagues.
 

About the department
The Injectable Finished Products (IFP) area produces high-quality products to fight diabetes and obesity worldwide. Site Support & Improvements (SSI) is a dynamic department in IFP Manufacturing Support, supporting our global IFP aseptic production sites and setting the direction for new technologies, innovation, and production optimization globally. We have a strong focus on making a difference in close collaboration with the IFP aseptic production sites, by implementing novel solutions based on data-driven decisions and in accordance with GMP regulations.


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